Label: CLEMENTINE HINT HAND SANITIZER- ethyl alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 24, 2021

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active Ingredients

    Ethanol: 70% v/v

  • Purpose

    Antiseptic

  • Use[s]

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    FLAMMABLE. Keep away from heat or flame. For external use only. Do not use on damaged or broken skin. Stop use and ask a doctor if irritation or rash occurs. When using this product, keep out of eyes, ears and mouth. Rinse with water to remove.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Place enough product on hands to cover all surfaces. Rub hands together until dry.
    Supervise children under 6 years of age when using this product to avoid swallowing.

  • Inactive ingredients

    Glycerin 1.45%, Hydrogen Peroxide 0.125%, Distilled Cold Water, Essential Oils

  • Other information

    Store between 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

  • Questions

    Call 866.895.4468

  • SPL UNCLASSIFIED SECTION

    Alcohol Antiseptic 70%

    Topical Solution

    Made in USA with US and Foreign materials.
    Distributed by: Hint, Inc.
    San Francisco, CA 94123

    www.drinkhint.com

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    CLEMENTINE HINT HAND SANITIZER 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81915-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    WATER (UNII: 059QF0KO0R)  
    MANDARIN OIL (UNII: NJO720F72R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81915-101-6060 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/15/2021
    Labeler - Hint, Inc. (612040142)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!